Browsing by Author Bailey, Charles
Showing results 1 to 3 of 3
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19
Author(s) | Seow, Heng; Broer, Stefan; Broer, Angelika, et al |
---|---|
Type | Journal article |
Date Published | 2004 |
Date Created | - |
Persistence of the Common Hartnup disease D173N Allele in populations of European origin
Author(s) | Azmanov, Dimitar; Rodgers, Helen; Auray-Blais, Christiane, et al |
---|---|
Type | Journal article |
Date Published | 2007 |
Date Created | - |
Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria
Author(s) | Vanslambrouck, Jessica M.; Broer, Angelika; Thavyogarajah, Thuvaraka, et al |
---|---|
Type | Journal article |
Date Published | 2010 |
Date Created | - |
- previous
- 1
- next
Updated: 12 April 2016/ Responsible Officer: University Librarian/ Page Contact: Library Systems & Web Coordinator